Canonical Allele Identifier: CA183221

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90855868G>A , CM000667.2:g.90855868G>A	GRCh38
NC_000005.9:g.90151685G>A , CM000667.1:g.90151685G>A	GRCh37
NC_000005.8:g.90187441G>A	NCBI36
NG_007083.1:g.302069G>A
NG_007083.2:g.331525G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17722G>A MANE Select	NP_115495.3:p.Ala5908Thr
ENST00000405460.9:c.17722G>A MANE Select	ENSP00000384582.2:p.Ala5908Thr
NM_032119.3:c.17722G>A	NP_115495.3:p.Ala5908Thr
NR_003149.1:n.17735G>A
NR_003149.2:n.17738G>A
ENST00000405460.6:c.17722G>A	ENSP00000384582.2:p.Ala5908Thr
ENST00000425867.2:c.4705G>A	ENSP00000392618.2:p.Ala1569Thr
ENST00000425867.3:c.6676G>A	ENSP00000392618.3:p.Ala2226Thr
ENST00000503852.1:n.270G>A
ENST00000638510.1:n.4989G>A
ENST00000638990.1:c.934G>A
ENST00000639431.1:c.266-129476G>A	ENSP00000491057.1:n.266-129476G>A
ENST00000640407.1:c.4171G>A	ENSP00000491425.1:n.4171G>A
XM_011543675.1:c.17719G>A	XP_011541977.1:p.Ala5907Thr
XM_011543676.1:c.17641G>A	XP_011541978.1:p.Ala5881Thr
XM_011543677.1:c.15025G>A	XP_011541979.1:p.Ala5009Thr
XM_017009963.2:c.17743G>A	XP_016865452.1:p.Ala5915Thr
XM_017009964.2:c.17740G>A	XP_016865453.1:p.Ala5914Thr
XM_017009965.1:c.17740G>A	XP_016865454.1:p.Ala5914Thr
XM_017009966.2:c.17662G>A	XP_016865455.1:p.Ala5888Thr
XM_017009967.1:c.17647G>A	XP_016865456.1:p.Ala5883Thr
XM_017009968.2:c.17563G>A	XP_016865457.1:p.Ala5855Thr
XM_017009969.2:c.17743G>A	XP_016865458.1:p.Ala5915Thr
XM_017009972.1:c.10861G>A	XP_016865461.1:p.Ala3621Thr
XM_017009973.1:c.10840G>A	XP_016865462.1:p.Ala3614Thr